Smith Sophia R, Ghosh Manik C, Ollivierre-Wilson Hayden, Hang Tong Wing, Rouault Tracey A
Section on Human Iron Metabolism, Cell Biology and Metabolism Branch National Institute of Child Health and Human Development Bethesda, MD 20892, USA.
Blood Cells Mol Dis. 2006 Mar-Apr;36(2):283-7. doi: 10.1016/j.bcmd.2005.12.006. Epub 2006 Feb 15.
Iron regulatory proteins 1 and 2 (IRPs) are homologous mammalian cytosolic proteins that sense intracellular iron levels and post-transcriptionally regulate expression of ferritin, transferrin receptor, and other iron metabolism proteins. Adult mice with homozygous targeted deletion of IRP2 develop microcytic anemia, elevated red cell protoporphyrin IX levels, high serum ferritin, and adult-onset neurodegeneration. Mice with homozygous deletion of IRP1 develop no overt abnormalities, but mice that lack both copies of IRP2 and one copy of IRP1 develop a more severe anemia and neurodegeneration than mice with deletion of IRP2 alone. Here, we have demonstrated that IRP1-/- IRP2-/- embryos do not survive gestation, and that although IRP1-/- IRP2-/blastocysts can be genotyped and harvested, implanted embryos with the IRP1-/- IRP2-/genotype are undetectable at embryonic day 6.5 and beyond. Blastocysts derived from a cross in which 25% of the fertilized embryos were expected to have the IRP1-/- IRP2-/genotype often showed brown discoloration and abnormal morphology. These abnormal blastocysts likely have the IRP1-/- IRP2-/- genotype, and the brown discoloration may be attributable to ferritin overexpression and sequestration of ferric iron in ferritin, whereas abnormal morphology may be due to concomitant functional iron deficiency. These results demonstrate that IRPs are indispensable for regulation of mammalian iron homeostasis at the post-implantation stage of murine embryonic development.
铁调节蛋白1和2(IRPs)是同源的哺乳动物胞质蛋白,可感知细胞内铁水平,并在转录后调节铁蛋白、转铁蛋白受体和其他铁代谢蛋白的表达。IRP2纯合靶向缺失的成年小鼠会出现小细胞贫血、红细胞原卟啉IX水平升高、血清铁蛋白升高以及成年期神经退行性变。IRP1纯合缺失的小鼠没有明显异常,但同时缺失IRP2的两个拷贝和IRP1的一个拷贝的小鼠,比仅缺失IRP2的小鼠出现更严重的贫血和神经退行性变。在这里,我们已经证明IRP1-/- IRP2-/-胚胎在妊娠期无法存活,并且尽管可以对IRP1-/- IRP2-/-囊胚进行基因分型和收获,但在胚胎第6.5天及以后无法检测到具有IRP1-/- IRP2-/-基因型的植入胚胎。来自杂交的囊胚,预计25%的受精胚胎具有IRP1-/- IRP2-/-基因型,常常表现出褐色变色和异常形态。这些异常囊胚可能具有IRP1-/- IRP2-/-基因型,褐色变色可能归因于铁蛋白过表达和铁蛋白中铁离子的螯合,而异常形态可能是由于伴随的功能性铁缺乏。这些结果表明,IRPs在小鼠胚胎发育的植入后阶段对调节哺乳动物铁稳态是不可或缺的。